| Organism name | Aglaonema spp. |
|---|---|
| Genus | Aglaonema |
| Family | Araceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Aglaonema |
|---|---|
| Linked NCBI taxonomy ID | 174181 |
| Linked level | genus |
| Family in NCBI taxonomy | Araceae |
|---|---|
| ID | 4454 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | Liliopsida |
|---|---|
| ID | 4447 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00002037
|
DMDP
/ (+)-2,5-Dideoxy-2,5-imino-D-mannitol / 2R,5R-Dihydroxymethyl-3R,4R-dihydroxy-pyrrolidine |
CHEMBL10437
CHEMBL312653 CHEMBL121093 CHEMBL259905 CHEMBL405957 CHEMBL469844 CHEMBL2008021 |
C043121
|
8 / 10 / 8 | No. 667 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00002037 | 6 / 4 |
| Q14697 | Neutral alpha-glucosidase AB | Enzyme | C00002037 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002037 | 1 / 1 |
| Q9H227 | Cytosolic beta-glucosidase | Enzyme | C00002037 | 0 / 0 |
| P35573 | Glycogen debranching enzyme | Enzyme | C00002037 | 1 / 1 |
| P04066 | Tissue alpha-L-fucosidase | Enzyme | C00002037 | 1 / 2 |
| P06280 | Alpha-galactosidase A | Enzyme | C00002037 | 1 / 1 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00002037 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #301500 | Fabry disease |
P06280
|
| #230000 | Fucosidosis |
P04066
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #232400 | Glycogen storage disease iii |
P35573
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| KEGG | name | UniProt |
|---|---|---|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00141 | Fucosidosis |
P04066
(related)
|
| H00422 | Glycoproteinoses |
P04066
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
P35573 (related) |